Skip to main content
Log in

Acetate-dependent photoheterotrophic growth and the differential requirement for the Calvin–Benson–Bassham reductive pentose phosphate cycle in Rhodobacter sphaeroides and Rhodopseudomonas palustris

  • Short Communication
  • Published:
Archives of Microbiology Aims and scope Submit manuscript

Abstract

Rhodobacter sphaeroides ribulose-1,5-bisphosphate carboxylase/oxygenase (RubisCO)-deletion strain 16 was capable of photoheterotrophic growth with acetate, while Rhodopseudomonas palustris RubisCO-deletion strain 2040 could not grow under these conditions. The reason for this difference lies in the fact that Rba. sphaeroides and Rps. palustris use different pathways for acetate assimilation, the ethylmalonyl-CoA pathway, and glyoxylate-bypass cycle, respectively. The ethylmalonyl-CoA pathway is distinct from the glyoxylate cycle as one molecule of CO2 and one molecule of HCO3 per three molecules of acetyl-CoA are co-assimilated to form two malate molecules. The glyoxylate cycle directly converts two acetyl-CoA molecules to malate. Each pathway, therefore, also dictates at what point, CO2 and reductant are consumed, thereby determining the requirement for the Calvin–Benson–Bassham reductive pentose phosphate cycle.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

References

  • Erb TJ, Berg IA, Brecht V, Müller M, Fuchs G, Alber BE (2007) Synthesis of C5-dicarboxylic acids from C2-units involving crotonyl-CoA carboxylase/reductase: the ethylmalonyl-CoA pathway. Proc Natl Acad Sci USA 104:10631–10636

    Article  CAS  PubMed  Google Scholar 

  • Fuchs G (1999) Biosynthesis of building blocks. In: Lengeler JW, Drews G, Schlegel HG (eds) Biology of the prokaryotes, Chap. 7. Thieme, Stuttgart, pp 114–116

    Google Scholar 

  • Kornberg HL, Lascelles J (1960) The formation of isocitratase by the Athiorhodaceae. J Gen Microbiol 23:511–517

    CAS  PubMed  Google Scholar 

  • Larimer FW, Chain P, Hauser L, Lamerdin J, Malfatti S, Do L, Land ML, Pelletier DA, Beatty JT, Lang AS, Tabita FR, Gibson JL, Hanson TE, Bobst C, Torres JL, Peres C, Harrison FH, Gibson J, Harwood CS (2004) Complete genome sequence of the metabolically versatile photosynthetic bacterium Rhodopseudomonas palustris. Nat Biotechnol 22:55–61

    Article  CAS  PubMed  Google Scholar 

  • McKinlay JB, Harwood CS (2010) Carbon dioxide fixation as a central redox cofactor recycling mechanism in bacteria. Proc Natl Acad Sci USA 107:11669–11675

    Article  CAS  PubMed  Google Scholar 

  • Meister M, Saum S, Alber BE, Fuchs G (2005) L-Malyl-coenzyme A/beta-methylmalyl-coenzyme A lyase is involved in acetate assimilation of the isocitrate lyase-negative bacterium Rhodobacter capsulatus. J Bacteriol 187:1415–1425

    Article  CAS  PubMed  Google Scholar 

  • Neidhardt FC, Ingraham JL, Schaechter M (1990) Biosynthesis and fueling. In: Physiology of the bacterial cell. Sinauer Associates, Inc., Sunderland, pp 133–172

    Google Scholar 

  • Ormerod JG, Ormerod KS, Gest H (1961) Light-dependent utilization of organic compounds and photoproduction of molecular hydrogen by photosynthetic bacteria; relationships with nitrogen metabolism. Arch Biochem Biophys 94:449–463

    Article  CAS  PubMed  Google Scholar 

  • Richardson DJ, King GF, Kelly DJ, McEwan AG, Ferguson SJ, Jackson JB (1988) The role of auxiliary oxidants in maintaining redox balance during growth of Rhodobacter capsulatus on propionate and butyrate. Arch Microbiol 150:131–137

    Article  CAS  Google Scholar 

  • Romagnoli S, Tabita FR (2006) A novel three-protein two-component system provides a regulatory twist on an established circuit to modulate expression of the cbb I region of Rhodopseudomonas palustris CGA010. J Bacteriol 188:2780–2791

    Article  CAS  PubMed  Google Scholar 

  • Tabita FR, Caruso P, Whitman W (1978) Facile assay of enzymes unique to the Calvin cycle in intact cells, with special reference to ribulose 1, 5-bisphosphate carboxylase. Anal Biochem 84:462–472

    Article  CAS  PubMed  Google Scholar 

  • Wang X, Falcone DL, Tabita FR (1993) Reductive pentose phosphate-independent CO2 fixation in Rhodobacter sphaeroides and evidence that ribulose bisphosphate carboxylase/oxygenase activity serves to maintain the redox balance of the cell. J Bacteriol 175:3372–3379

    CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We thank Trung Ho for assistance with the growth experiments. This work was supported by grants of the National Science Foundation MCB0842892, by a start-up fund from the Ohio State University (B. E. A.), and by grants DE-FG02-07ER64489 and DE-FG02-DE-FG02-08ER15976 from the Office of Biological and Environmental Research (Genomics: GTL Program) and the Chemical Sciences, Geosciences, and Biosciences Division of the Office of Basic Energy Sciences, respectively, of the U.S. Department of Energy (F. R. T.).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Birgit E. Alber.

Additional information

Communicated by Theo Hansen.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Laguna, R., Tabita, F.R. & Alber, B.E. Acetate-dependent photoheterotrophic growth and the differential requirement for the Calvin–Benson–Bassham reductive pentose phosphate cycle in Rhodobacter sphaeroides and Rhodopseudomonas palustris . Arch Microbiol 193, 151–154 (2011). https://doi.org/10.1007/s00203-010-0652-y

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00203-010-0652-y

Keywords

Navigation